FDA Adverse Event Other Summary report: N

DUROM HIP

MDR report key: 2135914 · Received June 14, 2011

Report

Report Number
9613350-2011-00346
Event Type
Other
Date Received
June 14, 2011
Report Date
May 12, 2011
Manufacturer
ZIMMER GMBH
Product Code
KWA
Removal / Correction Number
C9613350-07/15/2008-001
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

INFORMATION WAS FORWARDED FROM THE OWNER ESTABLISHMENT, ZIMMER INC., WHICH MARKETS THE DEVICES IN THE U.S. THE MANUFACTURER DID NOT RECEIVED EXPLANTED DEVICES, X-RAYS, OR OTHER SOURCE DOCUMENTS FOR REVIEW. WHERE LOT NUMBERS WERE RECEIVED FOR THE EXPLANTED DEVICES, THE DEVICE HISTORY RECORDS WERE REVIEWED AND FOUND TO BE CONFORMING. IT IS NOT SUSPECTED THAT DEVICE FAILURE HAS LEAD TO THE ALLEGED EVENT. WHILE A CAUSE FOR THIS SPECIFIC CLINICAL EVENT CANNOT BE ASCERTAINED FROM THE INFORMATION PROVIDED, THE COMMON CLINICAL PRESENTATION AND THE DATE OF THE ORIGINAL IMPLANTATION SUGGEST THAT THE REVISION SURGERY IS RELATED TO THE ISSUES FOR WHICH ZIMMER IMPLEMENTED A CORRECTION IN (B)(4) 2008. SHOULD ADDITIONAL INFORMATION BECOMES AVAILABLE AND/OR THE DEVICE(S) BE RETURNED FOR EVALUATION AND AN INVESTIGATION RESULT BE AVAILABLE, THAT CHANGES THIS ASSESSMENT, AN AMENDED MEDICAL DEVICE REPORT WILL BE FILED. THE NEED FOR FURTHER CORRECTIVE MEASURES IS NOT INDICATED AT THIS TIME AND ZIMMER GMBH CONSIDERS THIS CASE CLOSED. ZIMMER REFERENCE NUMBER OF THIS FILE IS (B)(4).

Description of Event or Problem · 1

IT IS REPORTED THAT PATIENT UNDERWENT TOTAL HIP ARTHROPLASTY ON (B)(6). IT IS ALSO REPORTED POST OP, PATIENT EXPERIENCED PAIN. PATIENT HAS NOT BEEN REVISED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DUROM HIP DUROM ACETABULAR COMPONENT AND METASUL KWA ZIMMER GMBH UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other